共 53 条
Plasminogen activator inhibitor 1 is an intracellular inhibitor of furin proprotein convertase
被引:36
作者:
Bernot, Denis
[1
]
Stalin, Jimmy
[1
]
Stocker, Pierre
[2
]
Bonardo, Bernadette
[1
]
Scroyen, Ilse
[1
]
Alessi, Marie-Christine
[1
]
Peiretti, Franck
[1
]
机构:
[1] Univ Aix Marseille 2, INSERM, Fac Med, U626, F-13385 Marseille 5, France
[2] Univ Paul Cezanne, Equipe Biosci iSm2 UMR 6263, FST St Jerome, F-13397 Marseille 20, France
关键词:
ADAM17;
Furin;
Golgi;
Insulin receptor;
PAI-1;
Convertase;
NECROSIS-FACTOR-ALPHA;
TRANSMEMBRANE TNF-ALPHA;
INSULIN-RESISTANCE;
ADIPOSE-TISSUE;
ENDOTHELIAL-CELLS;
SECRETORY PATHWAY;
ENDOGENOUS FURIN;
CUTTING EDGE;
ENZYME;
SERPIN;
D O I:
10.1242/jcs.079889
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
Proprotein convertases (PCs) are a family of serine proteases that are involved in the post-translational processing and activation of a wide range of regulatory proteins. The upstream role of PCs in the control of many physiological and pathological processes generates a growing interest in understanding their regulation. Here, we demonstrate that the serine protease inhibitor plasminogen activator inhibitor 1 (PAI-1) forms an SDS-stable complex with the PC furin, which leads to the inhibition of the intra-Golgi activity of furin. It is known that elevated PAI-1 plasma levels are correlated with the occurrence of the metabolic syndrome and type 2 diabetes, and we show that PAI-1 reduces the furin-dependent maturation and activity of the insulin receptor and ADAM17: two proteins involved in the onset of these metabolic disorders. In addition to demonstrating that PAI-1 is an intracellular inhibitor of furin, this study also provides arguments in favor of an active role for PAI-1 in the development of metabolic disorders.
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页码:1224 / 1230
页数:7
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